反応 #577243

ord-da4a91af0aa84ed989f93f5afd9145e1

反応方程式

NC(CO)(CO)CCc1ccc(OCc2ccccc2)cc1
2-amino-2-[2-(4-benzyloxy-phenyl)-ethyl]-propane-1,3-diol
CCC(CC)(CC)C([O-])([O-])[O-]
triethylortho acetate
CC(=O)O
acetic acid
CC1=NC(CO)(CCc2ccc(OCc3ccccc3)cc2)CO1
{4-[2-(4-benzyloxy-phenyl)-ethyl]-2-methyl-4,5-dihydro-oxazol-4-yl}-methanol

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮The reaction mixture is then concentrated under vacuum

実験手順

To a solution of 2-amino-2-[2-(4-benzyloxy-phenyl)-ethyl]-propane-1,3-diol (31.1 g, 0.10 mol) in acetonitrile (2.381) is added triethylortho acetate (17.1 ml, 0.12 mol, 1.2 eq) and acetic acid (5.48 ml, 0.11 mol, 1.1 eq), the reaction mixture is then stirred at 80° C. for 5 hours. The reaction mixture is then concentrated under vacuum, {4-[2-(4-benzyloxy-phenyl)-ethyl]-2-methyl-4,5-dihydro-oxazol-4-yl}-methanol is isolated after crystallization with ethyl acetate.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07528120B2uspto-grants-2009_05